Better Genomics
How are we delivering better genomics for the future? Exploring Long Read (RNA) sequencing, diverse data and the power of scale as tools to ensure equitable access.
Featuring speakers:
Dr Kate Downes, Rare Disease Lead Scientist, East Genomic Laboratory Hub @eastgenomics
Professor Matthew Hurles, Director and Senior Group Leader, Wellcome Sanger Institute @sangerinstitute
Professor Mina Ryten, Professor of Clinical Genetics, UCL Institute of Child Health
Matt Silver, Lead Genomic Data Scientist, @GenomicsEngland
Steven Hardy, Head of Genomics & Rare Disease, National Disease Registration Service
